Success in anaerobic culture closely depends on good conditions used in the
collection and transport of specimens. The importance of collecting specim
ens so as to avoid contamination with indigenous flora is emphasized. Speci
mens must be protected from the deleterious effects of oxygen until they ca
n be cultured. There is no specimen for which a swab is the ideal collectio
n process; only when no other options are available and the resulting infor
mation is judged to be important clinically should a swab be accepted for a
naerobic culture. Any aspirate material from a normally sterile body site i
s acceptable after skin preparation and disinfection. Pus and localized flu
id collection should be aspirated via needle and syringe. Then, a new steri
le needle, after pushing the air out, should be used to inject the material
into an anaerobic transport vial. When the site is difficult to puncture,
it is necessary to use a curette or vigorous swabbing to collect material f
rom below the surface after discarding contaminated surface tissues. Ca-alg
inate swabs must be used and should be placed immediately into an anaerobic
transport system. Any tissue or material obtained during surgery should be
appropriate for anaerobic culture placed into an anaerobic transport syste
m or sterile box if laboratory processing occurs within one to two hours. B
lood or infernal body fluids are injected directly into anaerobic blood cul
ture bottles. Specimens should be transported and held at room temperature;
refrigeration is unfavourable. The recovery of clinically significant anae
robes in well-collected and transported specimens is then possible if the l
aboratory uses appropriate anaerobic culture methods such as the anaerobic
chamber (C) 2000 Editions scientifiques et medicales Elsevier SAS.